GB458028A - Improvements in the manufacture and production of water-soluble condensation products having tanning action - Google Patents
Improvements in the manufacture and production of water-soluble condensation products having tanning actionInfo
- Publication number
- GB458028A GB458028A GB1635435A GB1635435A GB458028A GB 458028 A GB458028 A GB 458028A GB 1635435 A GB1635435 A GB 1635435A GB 1635435 A GB1635435 A GB 1635435A GB 458028 A GB458028 A GB 458028A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formaldehyde
- acid
- acids
- hydroxyphenyl
- cresol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C3/00—Tanning; Compositions for tanning
- C14C3/02—Chemical tanning
- C14C3/08—Chemical tanning by organic agents
- C14C3/18—Chemical tanning by organic agents using polycondensation products or precursors thereof
- C14C3/20—Chemical tanning by organic agents using polycondensation products or precursors thereof sulfonated
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Tanning-agents are prepared by condensing with formaldehyde and aromatic sulphonic acids, products obtained from insoluble substances having at least one phenolic hydroxy group and formaldehyde-bisulphite or formaldehyde and sulphurous acid salts. The tanning agents also have plumping action and may be used, after acidification with, for example, formic or sulphuric acid, for tanning reptile skins, unhaired hides or upper leathers. In modifications of the process of manufacture, (a) aromatic carboxylic acids are used instead of aromatic sulphonic acids; (b) hydroxy compounds of the benzene or naphthalene series are used with the aromatic sulphonic acids; (c) the products are further treated with urea and formaldehyde. In examples: (1) the product obtained by reacting together formaldehyde, calcined sodium sulphite and 4 : 4<1>-dihydroxydiphenylsulphone is condensed with formaldehyde and cresolsulphonic acid, b : b -di(4-hydroxyphenyl)propanesulphonic acid, a formaldehyde-cresolsulphonic acid condensation product, a formaldehyde-naphthalene sulphonic acid condensation product, a formaldehydecresolsulphonic acid condensation product together with cresol, b : b -di(4-hydroxyphenyl)-propane, or together with cresol and dihydroxydiphenylsulphone and b : b - di(4 - hydroxyphenyl)propanedisulphonic acid together with b : b -di(4-hydroxyphenyl)propane; (2) the product obtained by reacting together formaldehyde, calcined sodium sulphite and 4 : 4<1>-dihydroxy - 3 : 3<1> - dimethyldiphenylsulphone is condensed with formaldehyde and o-hydroxybenzoic acid; (3) the product obtained by reacting together formaldehyde, sodium sulphite and 4 : 4<1> - dihydroxy - 2 : 2<1> - dimethyldiphenylsulphone is condensed with formaldehyde and phthalic acid; (4) a product obtained by reacting together formaldehyde-bisulphite and humic acid is condensed with a formaldehyde-naphthalenesulphonic acid condensation product or a formaldehyde cresol sulphonic acid condensation product together with cresol or naphthol. Insoluble condensation products containing a phenolic hydroxy group obtained from phenol and formaldehyde, b : b -di(4-hydroxyphenyl)propane and humous coal may be reacted with formaldehydebisulphite and used as starting material. Condensation products of phenol, cresols and xylenols with aldehydes and ketones, dihydroxydiarylmethanes and dihydroxy diarylsulphides are also examples of insoluble phenolic compounds which may be used. The following aromatic sulphonic acids are mentioned: naphthalene mono and polysulphonic acids, chlorcresolsulphonic acids, sulphanilic acid, naphthylaminosulphonic acids and chlornaphthalenesulphonic acids. 4-Chlor-2-hydroxybenzoic acid, terephthalic acid, naphthalic acid and 2 : 2<1>-dihydroxydiphenyl methane-4 : 4<1>-dicarboxylic acid are specified carboxylic acids. According to the Provisional Specification any aldehyde or ketone of low molecular weight may replace the formaldehyde.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1635435A GB458028A (en) | 1935-06-05 | 1935-06-05 | Improvements in the manufacture and production of water-soluble condensation products having tanning action |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1635435A GB458028A (en) | 1935-06-05 | 1935-06-05 | Improvements in the manufacture and production of water-soluble condensation products having tanning action |
Publications (1)
Publication Number | Publication Date |
---|---|
GB458028A true GB458028A (en) | 1936-12-07 |
Family
ID=10075780
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1635435A Expired GB458028A (en) | 1935-06-05 | 1935-06-05 | Improvements in the manufacture and production of water-soluble condensation products having tanning action |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB458028A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3185666A (en) * | 1961-09-01 | 1965-05-25 | Union Carbide Corp | Phenol-aldehyde condensates containing hydroxybenzylated sulfones |
US3256361A (en) * | 1961-03-17 | 1966-06-14 | Union Carbide Corp | Sulfone containing phenolic resin compositions |
-
1935
- 1935-06-05 GB GB1635435A patent/GB458028A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3256361A (en) * | 1961-03-17 | 1966-06-14 | Union Carbide Corp | Sulfone containing phenolic resin compositions |
US3185666A (en) * | 1961-09-01 | 1965-05-25 | Union Carbide Corp | Phenol-aldehyde condensates containing hydroxybenzylated sulfones |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US1901536A (en) | Manufacture of tanning substances | |
US2099717A (en) | Process for the production of water-soluble condensation products | |
US2191943A (en) | Tanning material | |
US5733340A (en) | Aqueous composition for the pretanning of hide pelts or retanning of leather | |
US2112361A (en) | Synthetic tans and process of producing the same | |
US1539517A (en) | Process for tanning | |
US2621164A (en) | Preparation of sulfonated phenolic resins | |
GB458028A (en) | Improvements in the manufacture and production of water-soluble condensation products having tanning action | |
US3065039A (en) | Sulfo-methylated phenol-formaldehyde tanning agents | |
US2204512A (en) | Tanning material | |
US2282928A (en) | Water-soluble condensation products | |
US2122124A (en) | Water-soluble condensation products and a process of producing same | |
US2667466A (en) | Water soluble phenol-formaldehyde-borax condensation product | |
US1989802A (en) | Synthetic tanning material | |
US2218996A (en) | Tanning material | |
US2174287A (en) | Tanning agents and process of producing same | |
US2701749A (en) | Process of tanning with borated methylol phenols | |
GB465803A (en) | The manufacture of tanning materials | |
DE686111C (en) | Process for the production of water-soluble condensation products from lignosulfonic acids | |
US2316714A (en) | Leather treating agent | |
US2122125A (en) | Water-soluble condensation products and a process of producing same | |
US1972797A (en) | Tanning animal hides | |
DE707006C (en) | Process for the production of water-soluble condensation products | |
US1972798A (en) | Tanning animal hides | |
SU6662A1 (en) | The method of tanning skins or leather |